US6426352B1

US6426352B1 - Sulfonamide inhibitors of farnesyl-protein transferase

Info

Publication number: US6426352B1
Application number: US09/374,390
Authority: US
Inventors: F. George Njoroge; Bancha Vibulbhan; Arthur G. Taveras; Ronald J. Doll; Viyyoor M. Girijavallabhan
Original assignee: Schering Corp
Current assignee: Merck Sharp and Dohme Corp
Priority date: 1997-06-17
Filing date: 1999-08-13
Publication date: 2002-07-30
Anticipated expiration: 2018-06-15

Abstract

Novel tricyclic sulfonamide compounds and pharmaceutical compositions are disclosed which are inhibitors of the enzyme, farnesyl protein transferase. Also disclosed is a method of inhibiting Ras function and therefore inhibiting the abnormal growth of cells. The method comprises administering the novel sulfonamide compound to a biological system. In particular, the method inhibits the abnormal growth of cells in a mammals such as a human.

Description

REFERENCE TO RELATED APPLICATIONS

This is a continuation of Application Ser. No. 09/094,683 filed Jun. 15, 1998 (now abandoned) which in turn claims the benefit of U.S. Provisional Application 60/049,958 filed Jun. 17, 1997.

BACKGROUND

Patent application WO 95/00497 published Jan. 5, 1995 under the Patent Cooperation Treaty (PCT) describes compounds which inhibit the enzyme, farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. Oncogenes frequently encode protein components of signal transduction pathways which lead to stimulation of cell growth and mitogenesis. Oncogene expression in cultured cells leads to cellular transformation, characterized by the ability of cells to grow in soft agar and the growth of cells as dense foci lacking the contact inhibition exhibited by non-transformed cells. Mutation and/or overexpression of certain oncogenes is frequently associated with human cancer.

To acquire transforming potential, the precursor of the Ras oncoprotein must undergo farnesylation of the cysteine residue located in a carboxyl-terminal tetrapeptide. Inhibitors of the enzyme that catalyzes this modification, farnesyl protein transferase, have therefore been suggested as anticancer agents for tumors in which Ras contributes to transformation. Mutated, oncogenic forms of Ras are frequently found in many human cancers, most notably in more than 50% of colon and pancreatic carcinomas (Kohl et al., Science, Vol. 260, 1834 to 1837, 1993).

In view of the current interest in inhibitors of farnesyl protein transferase, a welcome contribution to the art would be additional compounds useful for the inhibition of farnesyl protein transferase. Such a contribution is provided by this invention.

SUMMARY OF THE INVENTION

Inhibition of farnesyl protein transferase by tricyclic compounds of this invention has not been reported previously. Thus, this invention provides a method for inhibiting farnesyl protein transferase using tricyclic compounds of this invention which: (i) potently inhibit farnesyl protein transferase, but not geranylgeranyl protein transferase I, in vitro; (ii) block the phenotypic change induced by a form of transforming Ras which is a farnesyl acceptor but not by a form of transforming Ras engineered to be a geranylgeranyl acceptor; (iii) block intracellular processing of Ras which is a farnesyl acceptor but not of Ras engineered to be a geranylgeranyl acceptor; and (iv) block abnormal cell growth in culture induced by transforming Ras.

This invention provides a method for inhibiting the abnormal growth of cells, including transformed cells, by administering an effective amount of a compound of this invention. Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g., loss of contact inhibition). This includes the abnormal growth of: (1) tumor cells (tumors) expressing an activated Ras oncogene; (2) tumor cells in which the Ras protein is activated as a result of oncogenic mutation in another gene; and (3) benign and malignant cells of other proliferative diseases in which aberrant Ras activation occurs.

Compounds useful in the claimed methods are represented by Formula 1.0:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

A represents N or N-oxide;

X represents N, CH or C, such that when X is N or CH, there is a single bond to carbon atom 11 as represented by the solid line; or when X is C, there is a double bond to carbon atom 11, as represented by the solid and dotted lines;

X¹and X²are independently selected from bromo, iodo or chloro;

X3 and X⁴are independently selected from bromo, iodo, chloro, fluro or hydrogen provided only one of X³or X⁴is hydrogen;

R⁵, R⁶, R⁷and R⁸each independently represents hydrogen, alkyl, aryl, or —CONR²⁰R²¹wherein R²⁰and R²¹independently represent hydrogen, alkyl, alkoxy, aryl, aralkyl, heteroaryl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl and heterocycloalkylalkyl, and further wherein R⁵may be combined with R⁶to represent ═O or ═S and/or R⁷may be combined with R⁸to represent ═O or ═S;

R can represent alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl or —NR¹⁰R¹¹,

wherein R¹⁰and R¹¹can independently represent hydrogen, alkenyl, alkyl, aryl, aralkyl, heteroaryl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl or heterocycloalkylalkyl.

Preferably in compound (1.0), there is a single bond at carbon atom 11; X is CH; R⁵, R⁶, R⁷and R⁸are hydrogen; X¹, X²and X³are bromo or chloro and X⁴is hydrogen; and R is alkyl, trifluoromethyl, alkenyl, aryl, hetemaryo or —NR¹⁰R¹¹wherein R¹⁰and R¹¹are independently selected from hydrogen and alkyl. When R is alkyl, an optional substituent on the alkyl group may be trifluoromethyl. When R is heteroaryl, optional substituents on the heteroaryl group may include alkyl or heteroaryl. Preferred compounds include those of Examples 1, 3, 4, 5, 6, 9, 10, 11 and 13.

In another embodiment, the present invention is directed toward a pharmaceutical composition for inhibiting the abnormal growth of cells comprising an effective amount of compound (1.0) in combination with a pharmaceutically acceptable carrier.

In another embodiment, the present invention is directed toward a method for inhibiting the abnormal growth of cells, including transformed cells, comprising administering an effective amount of compound (1.0) to a mammal (e.g., a human) in need of such treatment. Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g., loss of contact inhibition). This includes the abnormal growth of: (1) tumor cells (tumors) expressing an activated Ras oncogene; (2) tumor cells in which the Ras protein is activated as a result of oncogenic mutation in another gene; (3) benign and malignant cells of other proliferative diseases in which aberrant Ras activation occurs, and (4) benign or malignant cells that are activated by mechanisms other than the Ras protein. Without wishing to be bound by theory, it is believed that these compounds may function either through the inhibition of G-protein function, such as ras p21, by blocking G-protein isoprenylation, thus making them useful in the treatment of proliferative diseases such as tumor growth and cancer, or through inhibition of ras famesyl protein transferase, thus making them useful for their antiproliferative activity against ras transformed cells.

The cells to be inhibited can be tumor celis expressing an activated ras oncogene. For example, the types of cells that may be inhibited include pancreatic tumor cells, lung cancer cells, myeloid leukemia tumor cells, thyroid follicular tumor cells, myelodysplastic tumor cells, epidermal carcinoma tumor cells, bladder carcinoma tumor cells, prostate tumor cells, breast tumor cells or colon tumors cells. Also, the inhibition of the abnormal growth of cells by the treatment with compound (1.0) may be by inhibiting ras farnesyl protein transferase. The inhibition may be of tumor cells wherein the Ras protein is activated as a result of oncogenic mutation in genes other than the Ras gene. Alternatively, compounds (1.0) may inhibit tumor cells activated by a protein other than the Ras protein.

This invention also provides a method for inhibiting tumor growth by administering an effective amount of compound (1.0) to a mammal (e.g., a human) in need of such treatment. In particular, this invention provides a method for inhibiting the growth of tumors expressing an activated Ras oncogene by the administration of an effective amount of the above described compounds. Examples of tumors which may be inhibited include, but are not limited to, lung cancer (e.g., lung adenocarcinoma), pancreatic cancers (e.g., pancreatic carcinoma such as, for example, exocrine pancreatic carcinoma), colon cancers (e.g., colorectal carcinomas, such as, for example, colon adenocarcinoma and colon adenoma), myeloid leukemias (for example, acute myelogenous leukemia (AML)), thyroid follicular cancer, myelodysplastic syndrome (MDS), bladder carcinoma, prostate carcinoma and breast carcinoma and epidermal carcinoma.

It is believed that this invention also provides a method for inhibiting proliferative diseases, both benign and malignant, wherein Ras proteins are aberrantly activated as a result of oncogenic mutation in other genes—i.e., the Ras gene itself is not activated by mutation to an oncogenic form—with said inhibition being accomplished by the administration of an effective amount of the N-substituted urea compounds (1.0) described herein, to a mammal (e.g, a human) in need of such treatment. For example, the benign proliferative disorder neurofibromatosis, or tumors in which Ras is activated due to mutation or overexpression of tyrosine kinase oncogenes (e.g., neu, src, abl, Ick, and fyn), may be inhibited by the N-substituted urea compounds (1.0).

In another embodiment, the present invention is directed toward a method for inhibiting ras farnesyl protein transferase and the farnesylation of the oncogene protein Ras by administering an effective amount of compound (1.0) to mammals, especially humans. The administration of the compounds of this invention to patients, to inhibit farnesyl protein transTerase, is useful in the treatment of the cancers described above.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, the following terms are used as defined below unless otherwise indicated:

M⁺-represents the molecular ion of the molecule in the mass spectrum;

MH⁺-represents the molecular ion plus hydrogen of the molecule in the mass spectrum;

Bu-represents butyl;

Et-represents ethyl;

Me-represents methyl;

Ph-represents phenyl;

benzotriazol-1-yloxy represents

1-methyl-tetrazol-5-ylthio represents

alkyl-(including the alkyl portions of alkoxy, alkylamino and dialkylamino)-represents straight and branched carbon chains and contains from one to twenty carbon atoms, preferably one to six carbon atoms; for example methyl, ethyl, propyl, iso-propyl, n-butyl, t-butyl, n-pentyl, isopentyl, hexyl and the like; wherein said alkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²can independently represent hydrogen, alkyl, alkoxy, aryl, aralkyl, heteroaryl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl or heterocycloalkylalkyl;

alkenyl—represents straight and branched carbon chains having at least one carbon to carbon double bond and containing from 2 to 12 carbon atoms, preferably from 2 to 6 carbon atoms and most preferably from 3 to 6 carbon atoms; wherein said alkenyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, alkoxy, amino, alkylamino, cyano, —CF₃, dialkylamino, hyciroxy, oxy, phenoxy, —OCF₃, heterocycloalkyl, —SO₂NH₂, —NHSO₂R¹⁰, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰, —NCOR¹⁰or —COOR¹⁰;

alkoxy-an alkyl moiety of one to 20 carbon atoms covalently bonded to an adjacent structural element through an oxygen atom, for example, methoxy, ethoxy, propoxy, butoxy, pentoxy, hexoxy and the like; wherein said alkoxy group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

aryl (including the aryl portion of arylalkyl)-represents a carbocyclic group containing from 6 to 15 carbon atoms and having at least one aromatic ring (e.g., aryl is phenyl), wherein said aryl group optionally can be fused with aryl, cycloalkyl, heteroaryl or heterocycloalkyl rings; and wherein any of the available substitutable carbon and nitrogen atoms in said aryl group and/or said fused ring(s) may be optionally and independently substituted with one, two,. three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R10 and R¹²are as defined hereinabove;

arylalkyl—represents an alkyl group, as defined above, wherein one or more hydrogen atoms of the alkyl moiety have been substituted with one or more aryl groups; wherein said aralkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

aryloxy—represents an aryl group, as defined above. wherein said aryl group is covalently bonded to an adjacent structural element through an oxygen atom, for example, phenoxy, wherein said aryl group optionally can be fused with aryl, cycloalkyl, heteroaryl or heterocycloalkyl rings; and wherein any of the available substitutable carbon and nitrogen atoms in said aryloxy group and/or said fused ring(s) may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR10, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

cycloalkyl—represents saturated carbocyclic rings branched or unbranched of from 3 to 20 carbon atoms, preferably 3 to 7 carbon atoms; wherein said cycloalkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

cycloalkylalkyl—represents an alkyl group, as defined above, wherein one or more hydrogen atoms of the alkyl moiety have been substituted with one or more cycloalkyl groups; wherein said cycloallkylalkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

halo—represents fluoro, chloro, bromo and iodo;

heteroalkyl—represents straight and branched carbon chains containing from one to twenty carbon atoms, preferably one to six carbon atoms interrupted by 1 to 3 heteroatoms selected from —O—, —S— and —N—; wherein any of the available substitutable carbon and nitrogen atoms in said heteroalkyl chain may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R12 are as defined hereinabove;

heteroaryl—represents cyclic groups having at least one heteroatom selected from O, S and N, said heteroatom(s) interrupting a carbocyclic ring structure and having a sufficient number of delocalized pi electrons to provide aromatic character, with the aromatic heterocyclic groups containing from 2 to 14 carbon atoms,wherein said heteroaryl group optionally can be fused with one or more aryl, cycloalkyl, heteroaryl or heterocycloalkyl rings; and wherein any of the available substitutable carbon or nitrogen atoms in said heteroaryl group and/or said fused ring(s) may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR10, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove.

Representative heteroaryl groups can include, for example, furanyl, imidazoyl, pyrimidinyl, triazolyl, 2-, 3- or 4-pyridyl or 2-, 3- or 4-pyridyl N-oxide wherein pyridyl N-oxide can be represented as:

heteroarylalkyl—represents an alkyl group, as defined above, wherein one or more hydrogen atoms have been replaced by one or more heteroaryl groups; wherein said heteroarylalkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove;

heterocycloalkyl—represents a saturated, branched or unbranched carbocylic ring containing from 3 to 15 carbon atoms, preferably from 4 to 6 carbon atoms, which carbocyclic ring is interrupted by 1 to 3 heteroatoms selected from —O—, —S— and —N—, wherein optionally, said ring may contain one or two unsaturated bonds which do not impart aromatic character to the ring; and wherein any of the available substitutable carbon and nitrogen atoms in the ring may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰R¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove. Representative heterocycloalkyl groups can include 2- or 3-tetrahydrofuranyl, 2- or 3- tetrahydrothienyl, 1-, 2-, 3- or 4-piperidinyl, 2- or 3-pyrrolidinyl, 1-, 2- or 3-piperizinyl, 2- or 4-dioxanyl, morpholinyl,

or

wherein R¹⁰is defined hereinbefore and t is 0, 1 or 2.

heterocycloalkalkyl—represents an alkyl group, as defined above, wherein one or more hydrogen atoms have been replaced by one or more heterocycloalkyl groups; wherein optionally, said ring may contain one or two unsaturated bonds which do not impart aromatic character to the ring; and wherein said heterocycloalkylalkyl group may be optionally and independently substituted with one, two, three or more of the following: halo, alkyl, aryl, cycloalkyl, cyano, —CF₃, oxy (═O), aryloxy, —OR¹⁰, —OCF₃, heterocycloalkyl, heteroaryl, —NR¹⁰OR¹², —NHSO₂R¹⁰, —SO₂NH₂, —SO₂NHR¹⁰, —SO₂R¹⁰, —SOR¹⁰, —SR¹⁰, —NHSO₂, —NO₂, —CONR¹⁰R¹², —NR¹²COR¹⁰, —COR¹⁰, —OCOR¹⁰, —OCO₂R¹⁰or —COOR¹⁰, wherein R¹⁰and R¹²are as defined hereinabove.

The following solvents and reagents are referred to herein by the abbreviations indicated: tetrahydrofuran (THF); ethanol (EtOH); methanol (MeOH); acetic acid (HOAc or AcOH); ethyl acetate (EtOAc); N,N-dimethylformamide (DMF); trifluoroacetic acid (TFA); trifluoroacetic anhydride (TFAA); 1-hydroxybenzotriazole (HOBT); m-chloroperbenzoic acid (MCPBA); triethylamine (Et₃N); diethyl ether (Et₂O); ethyl chloroformate (ClCO₂Et); and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (DEC).

Reference to the position of the substituents X¹, X², X³and X⁴is based on the numbered ring structure:

Certain compounds of the invention may exist in different stereoisomeric forms (e.g., enantiomers, diastereoisomers and atropisomers). The invention contemplates all such stereoisomers both in pure form and in mixture, including racemic mixtures. For example, the carbon atom at the C-11 position can be in the S or R stereoconfiguration.

Certain tricyclic compounds will be acidic in nature, e.g. those compounds which possess a carboxyl or phenolic hydroxyl group. These compounds may form pharmaceutically acceptable salts. Examples of such salts may include sodium, potassium, calcium, aluminum, gold and silver salts. Also contemplated are salts formed with pharmaceutically acceptable amines such as ammonia, alkyl amines, hydroxyalkylamines, N-methylglucamine and the like.

Certain basic tricyclic compounds also form pharmaceutically acceptable salts, e.g., acid addition salts. For example, the pyrido-nitrogen atoms may form salts with strong acid, while compounds having basic substituents such as amino groups also form salts with weaker acids. Examples of suitable acids for salt formation are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic and other mineral and carboxylic acids well known to those skilled in the art. The salts are prepared by contacting the free base form with a sufficient amount of the desired acid to produce a salt in the conventional manner. The free base forms may be regenerated by treating the salt with a suitable dilute aqueous base solution such as dilute aqueous NaOH, potassium carbonate, ammonia and sodium bicarbonate. The free base forms differ from their respective salt forms somewhat in certain physical properties, such as solubility in polar solvents, but the acid and base salts are otherwise equivalent to their respective free base forms for purposes of the invention.

All such acid and base salts are intended to be pharmaceutically cceptable salts within the scope of the invention and all acid and base salts are onsidered equivalent to the free forms of the corresponding compounds for urpopses of the invention.

Compounds of the present invention can be prepared according to the following Scheme 1:

wherein X, X¹, X², X³, X⁴, R, R⁵, R⁶, R⁷, R⁸, and the solid and dotted lines are as defined hereinbefore.

Referring to the Scheme I, compounds of formula (1.0) can be prepared by reacting the compound of formula (5.0, 5.01, 6.0 or 10.9) with the corresponding sulfonyl chloride reagent of formula (2.6) with a base and aprotic solvent such as THF, dioxane, toluene, methylene chloride (CH₂Cl₂), acetonitrile, or DMF at temperatures which can range from 0° to 100° C., or reflux of the reaction mixture. The amount of sulfonyl chloride (2.6) can range from 1 to about 10 moles per mole of compound (5.0, 5.01, 6.0 or 10.9).

In an alternative procedure, the compounds of formula (1.0) wherein R is —NR¹⁰R¹¹can be prepared by reacting the compound of formula (5.0, 5.01, 6.0 or 10.9) with thionyl chloride in an aprotic solvent as described above, in the presence of a base, followed by reaction with an amine of the formula HNR¹⁰R¹¹(2.8) in an aprotic solvent wherein R¹⁰and R¹¹are defined hereinbefore, at a temperatures from 0° to 100° C. or reflux of the reaction mixture. The amount of the thionyl chloride or amine (2.8) can range from about 1 to 10 moles per mole of compound (5.0, 5.01, 6.0 or 10.9).

In another alternative procedure, the compounds of formula (1.0) wherein R is —NH₂can be prepared by reacting compound (2.0) with the sulfonamide SO(NH₂)₂in a protic solvent such as water at temperatures ranging from 50° to 100° C.

Compounds of fomula (1.0) can be isolated from the reaction mixture using conventional procedures, such as, for example, extraction of the reaction mixture from water with organic solvents, evaporation of the organic solvents, followed by chromatography on silica gel or other suitable chromatographic media. Alternatively, compounds (1.0) can be dissolved in a water-miscible solvent, such as methanol, the methanol solution is added to water to precipitate the compound, and the precipitate is isolated by filtration or centrifugation.

(+)-Isomers of compounds of formula (5.0, 6.0 and 10.9) wherein X is CH can be prepared with high enantioselectivity by using a process comprising enzyme catalyzed transesterification. Preferably, a racemic compound of formula (5.0, 6.0 and 10.9), wherein X is C, the double bond is present and X³is not H, is reacted with an enzyme such as Toyobo LIP-300 and an acylating agent such as trifluoroethly isobutyrate; the resultant (+)-amide is then hydrolyzed, for example by refluxing with an acid such as H₂SO₄, to obtain the corresponding optically enriched (+)-isomer wherein X is CH and R³is not H. Alternatively, a racemic compound of formula (5.0, 6.0 and 10.9), wherein X is C, the double bond is present and R³is not H, is first reduced to the corresponding racemic compound of formula (5.0, 6.0 and 10.9) wherein X is CH and then treated with the enzyme (Toyobo LIP-300) and acylating agent as described above to obtain the (+)-amide, which is hydrolyzed to obtain the optically enriched (+)-isomer.

Compounds of the present invention and preparative starting materials thereof, are exemplified by the following examples, which should not be construed as limiting the scope of the disclosure.

EXAMPLE 1 (+)-4-(3-Bromo-8,10-dichloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(methylsulfonyl)pipiridine

Dry anhydrous potassium carbonate (0.23 g, 1.7 mmnol) was suspended in 6 mL of anhydrous toluene. To this mixture was added the title compound of Preparative Example 10 (0.2 g, 0.47 mmol), methane sulfonyl chloride (0.055 g, 40 μL, 0.47 mmol) and stirred at room temperature for ˜72 h. The reaction mixture was then filtered, and washed with CH₂Cl₂. The filtrate was washed with saturate NaHCO₃, dried over MgSO4, filtered and concentrated to dryness to afford 0.23 g of the title compound as a white solid: mp=160-163° C., FAB-MS: MH⁺=505 (97% Yield), COS IC₅₀=0.420 (μM).

EXAMPLE 2 (+)-4-(3-Bromo-8,10-dichloro-6,11-dihydro-5H-benzo[5,6,]cyclohepta[1,2-b]pyridin-11-yl)-N-N-dimethyl-1-piperidinesulfonamide

The title compound is prepared following essentially the same procedure as described in Example 1 except that N,N-dimethyl sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid, FAB-MS: MH⁺=534, mp=202-203° C.; (65% Yield).

EXAMPLE 3 (+)-4-(3-Bromo-8,10-dichloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(aminosulfonyl)piperidine

The title compound of Preparative Example 10 (0.2 g, 0.47 mmol), and sulfamide (0.45 g, 4.7 mmol) are dissolved in 7 mL of H2O and the reaction mixture heated to reflux for 72h. The reaction mixure was then cooled and filtered. The filtrate was extracted with CH₂Cl₂, dried over MgSO4 and concentrated. Purification by flash chromatography on silica gel eluting with 5% MeOH(sat. with ammionia)-CH₂Cl₂afforded 0.035 g (15% yield) of the title compound, as a white solid. FAB-MS: MH⁺=506. mp=133-134° C.

EXAMPLE 4 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(methylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 1 except that the title compound of Preparative Example 3 (+)-4-(3,10-dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclo-hepta[1,2-b]pyridin-11-yl)-1-pipiridine) was used instead of (+)-4-(3-bromo-8,10-dichloro-6,11-dihydro-5H-benzo[5,6]cyclo-hepta[1,2-b]pyridin-11-yl)-1-pipiridine to obtain the title compound, a solid. FAB-MS: MH⁺=549, mp=216-217° C., yield=74%, COS IC₅₀=0.015 (μM).

EXAMPLE 5 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(ethylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that ethane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=563. mp=202-203° C. yield=90%

EXAMPLE 6 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(propylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that propane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=577. mp=97-98° C. yield=95%

EXAMPLE 7 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(isopropylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that isopropane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=577. mp=203-205° C. (yield=65%).

EXAMPLE 8 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(butylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that butane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=591. mp=73-74° C. yield=28%

EXAMPLE 9 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(trifluoromethyl sulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that trifluoromethane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=603. mp=111-112° C. yield=47%

EXAMPLE 10 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(trifluoroethyl sulfonyl)pipiridine

The title compound is prepared following essentially the same procedure as described in Example 4 except that trifluoroethane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=617. mp=174-175° C. yield=46%

EXAMPLE 11 (+)-4-(3,10-Dibromo-8-chloro-11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-1-(vinylsulfonyl)pipiridine

The title compound is prepared following essentially the same procedurie as described in Example 4 except that 2-chloro-ethane sulfonyl chloride was used instead of methane sulfonyl chloride to obtain a solid FAB-MS: MH⁺=514. mp=129-130° C. yield=35%

EXAMPLE 12 (+)-4-(3,10-Dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(R)-yl)-1-(phenylsulfonyl)pipiridine

To the title compound of Preparative Example 3 (0.05 g, 0.11 mmol) and triethylamine (0.015 mL, 1.5 eq) dissolved in anhydrous dichloromethane (10 mL) was added benzenesulfonyl chloride (0.015 mL, 1.1 eq). After stirring at room temperature overnight, the solution was diluted with dichloromethane, washed with 1 M hydrochloric acid, then washed with 1 N aqueous sodium hydroxide and dried over anhydrous magnesium sulfate. Filtration and concentration in vacuo afforded the title compound (0.064 g, 99% yield, mp=124.3-129° C.).

EXAMPLE 13 (+)-4-(3,10-Dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(R)-yl)-1-[(1-methyl-1H-imidazol-4-yl)sulfonyl]pipiridine

To the title compound of Preparative Example 3 (0.05 g, 0.11 mmol) and triethylamine (0.015 mL, 1.5 eq) dissolved in anhydrous dichloromethane (10 mL) was added 1-methylimidazole-4-sulfonyl chloride (0.021 g, 1.1 eq). After stirring at room temperature overnight, the solution was diluted with dichloromethane, washed with 1 M hydrochloric acid, then washed with 1 N aqueous sodium hydroxide and dried over anhydrous magnesium sulfate. Filtration and concentration in vacuo afforded the title compound (0.054 g, 82% yield, mp 157.5-161.2° C.).

EXAMPLE 14 (+)-4-(3,10-Dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(R)-yl)-1-[(5-(3-isoxazolyl)-2-thienyl]sulfonyl]pipiridine

To the title compound of Preparative Example 3 (0.05 g, 0.11 mmol) and triethylamine (0.015 mL, 1.5 eq) dissolved in anhydrous dichloromethane (10 mL) was added 5-(isoxazol-3-yl)thiophen-2-sulfonyl chloride (0.029 g, 1.1 eq). After stirring at room temperature overnight, the solution was diluted with dichloromethane, washed with 1 M hydrochloric acid, then washed with 1 N aqueous sodium hydroxide and dried over anhydrous magnesium sulfate. Filtration and concentration in vacuo afforded the title compound (0.069 g, 94%, mp 131.7-134.8° C.).

PREPARATION OF STARTING MATERIALS

Starting materials useful in preparing the compounds of the present invention are exemplified by the following preparative examples, which should not be construed to limit the scope of the disclosure. The tricylic compounds used as starting materials, such as compound (11.0), inorganic and organic bases, and alcohols can be prepared using known methods in the art, such as taught in See J. K. Wong et al., Bioorganic & Medicinal Chemistry Letters, Vol. 3, No. 6, pp. 1073-1078, (1993); U.S. Pat. Nos. 5,089,496; 5,151,423; 4,454,143; 4,355,036; PCT/US94/11390 (WO95/10514); PCT/US94/11391 (WO 95/10515); PCT/US94/11392 (WO95/10516); Stanley R. Sandler and Wolf Karo, Organic Functional Group Preparations, 2nd Edition, Academic Press, Inc., San Diego, Calif., Vol.1-3, (1983), and in J. March, Advanced Organic Chemistry, Reactions & Mechanisms, and Structure, 3rd Edition, John Wiley & Sons, New York, 1346 pp. (1985). Alternative mechanistic pathways and analogous structures within the scope of the invention may be apparent to those skilled in the art.

Starting materials used to prepare the compounds of the present invention are depicted in Scheme IV:

wherein for Scheme IV,

A, X, X₁, X², X³, R, Z, R⁵, R⁶, R⁷and R⁸the solid and dotted lines are as defined hereinbefore; and R¹⁵can represent any of the values for R¹⁰or R¹²as defined hereinbefore.

In Step A (Scheme IV), compounds of formula (10.0) can be prepared by reacting the compounds of formula (11.0) with a nitrating agent and/or optional protic or aprotic solvent such as those described hereinbefore. In a first procedure, compound (11.0) is reacted with about an equimolar amount of a nitrate salt, such as potassium nitrate, and acid, such as sulfuric acid at temperatures ranging from about −20° to +5° C. In a second procedure, compound (11.0) is treated with a mixture comprised of about two equivalents of trifluoromethanesulfonic acid and about one equivalent nitric acid in a solvent such as trifluoromethanesulfonic acid. In a third procedure, compound (11.0) is treated with a mixture comprised of about one equivalent of fuming nitric acid and about ten equivalents of trifluoromethanesulfonic anhydride in a solvent such as nitromethane. In a fourth procedure, compound (11.0) is treated with a nitronium salt, such as nitronium tetrafluoroborate, in a solvent, such as sulfolane. In a fifth procedure, compound (11.0) is reacted with fuming nitric acid at temperatures ranging from about −20° to +50° C.

In Step B (Scheme IV), compounds of formula (9.0) can be prepared by reacting compounds of the formula (10.0) with a reducing agent. In a first procedure, compound (10.0) can be reacted with about ten equivalents of a metal, such as iron, in a solvent, such as ethanol, in the presence of a salt, such as calcium chloride, at temperatures ranging from about 0° to +80° C. In a second procedure, compound (10.0) can be reacted with about ten equivalents of a metal, such as zinc, in a solvent, such as ethanol, in the presence of an acid, such as acetic acid at temperatures ranging from about 0° to +80° C. In a third procedure, compound (10.0) can be reacted with about five equivalents; of stannous chloride hydrate in a solvent, such as ethyl acetate. In a fourth procedure, compound (10.0) can be reacted with about ten equivalents of a metal, such as tin, in a solvent, such as ethanol, in the presence of an acid, such as hydrochloric acid.

In Step C (Scheme IV), compounds of formula (8.0) can be prepared by reacting compounds of the formula (9.0) with a halogenating agent. In a first procedure, compound (9.0) can be reacted with an excess of an elemental halogen, such as bromine, in a suitable solvent, such as acetic acid at temperatures ranging from about 0° to 20° C. In a second procedure, compound (9.0) can be reacted with a salt, such as pyridinium bromide perbromide, in a solvent, such as THF, at temperatures from about 0° to +40° C. In a third procedure, compound (9.0) can be reacted with a halogen, such as chlorine, in the presence of a Lewis acid, such as iron(III) chloride, in a suitable solvent, such as dichloromethane.

In Step D (Scheme IV), compounds of formula (7.0) can be prepared by reacting compounds of the formula (8.0) with an oxidizing agent followed by a reducing agent, or by reacting compounds of the formula (8.0) with an oxidizing agent in the presence of a hydrogen atom source. In a first procedure, compound (8.0) can be reacted with a diazotizing agent, such as t-butyl nitrite, in a solvent and hydrogen atom source, such as DMF at temperatures from about 0° to +100° C. In a second procedure, compound (8.0) can be reacted with a diazotizing agent, such as sodium nitrite, and an acid, such as hydrochloric acid, and a reducing agent, such as hypophosphorous acid at temperatures from about −15° to +50° C. In a third procedure, compound (8.0) can be reacted with a diazotizing agent, such as sodium nitrite, and an acid, such as aqueous sulfuric acid, followed by treatment with a metal, such as copper. In a fourth procedure, compound (8.0) can be reacted with a diazotizing agent, such as sodium nitrite, and an acid, such as fluoboric acid, followed by treatment with a reducing agent, such as sodium borohydride.

In Step E (Scheme IV), compounds of formula (6.0) can be prepared by reacting compounds of the formula (7.0) under hydrolysis conditions. In a first procedure, compound (7.0) can be reacted with an acid, such as hydrochloric acid, at temperatures from about 20° to +90° C. In a second procedure, compound (7.0) can be reacted with a base, such as aqueous sodium hydroxide, in a suitable solvent, such as ethanol, at temperatures from about 20° to +90° C. In a third procedure, compound (7.0) can be reacted with a nucleophile, such as hydrazine hydrate, in a solvent, such as ethanol, with an optional base, such as sodium hydroxide, at temperatures from about 20° to +90° C. In a fourth procedure, compound (7.0) can be reacted with a silyl chloride, such as trimethylsilyl chloride, in a solvent, such as THF or CH₂Cl₂at temperatures ranging from about 0° C. to reflux. In a fifth procedure, compound (7.0) can be reacted with an acid, such as trifluoroacetic acid, in an aprotic solvent, such as CH₂Cl₂.

In Step F (Scheme IV), compounds of formula (5.0) wherein X=CH can be prepared by reacting compounds of the formula (6.0) under reducing conditions. Compound (6.0) can be reacted with an alkyl-metal hydride, such as diisobutyl aluminum hydride or lithium aluminum hydride (LAH), in a solvent, such as toluene or THF, at temperatures from about 0° to +90° C.

In Step G (Scheme IV), compounds of formula (1.0) can be prepared as described previously for Scheme I.

In Step K (Scheme IV), compounds of formula (6.1) can be prepared by reacting the compound of formula (5.9) with a nitrating agent and/or optional protic or aprotic solvent according to the procedures described in Step A (Scheme IV).

In Step L (Scheme IV), compounds of formula (6.2) can be prepared by reacting the compound of formula (6.1) with a reducing agent according to the procedures described in Step B (Scheme IV).

In Step M (Scheme IV), compounds of formula (6.31) can be prepared by reacting the compound of formula (6.2) with a halogenating agent according to the procedures described in Step C (Scheme IV).

In Step N (Scheme IV), compounds of formula (6.3) can be prepared by reacting the compound of formula (6.31) with an oxidizing agent followed by a reducing agent, or by reacting compounds of the formula (6.31) with an oxidizing agent in the presence of a hydrogen atom source according to the procedures described in Step D (Scheme IV).

In Step O (Scheme IV), compounds of formula (6.5) can be prepared by reacting compounds of formula (6.3) with sodium borohydride (NaBH₄) in a solvent such as ethanol/toluene under reflux conditions for 10 minutes or at 25° C. for two hours or more.

In Step P (Scheme IV), compounds of formula (6.7) can be prepared by reacting compounds of formula (6.5) with SOCl₂in a solvent such as CH₂Cl₂at a temperature of about 25° C. for about 4 hours or more.

In Step Q (Scheme IV), compounds of formula (5.0) wherein X=N, can be prepared by reacting compounds (6.7) with an excess amount of the piperazine compound of formula (6.9) in a solvent such as THF at 25° C. or reflux for one hour or more.

Additional starting materials which can be used to prepare the compounds of the present invention are depicted in Scheme V.

In Step A (Scheme V), compounds of fomula (10.0) can be prepared from compound of formula (11.0) using the procedures described in Scheme IV, Step A.

In Step AA(Scheme V), compounds of formula (10.3) can be prepared by reacting compound of formula (10.0) with 1,3-dibromo-5,5-dimethylhydantoin in an acid, such as trifluoromethane sulfonic acid or sulfuric acid for about 24 h or more at 25° C.

In Step BB (Scheme V), compounds of the formula (10.5) can be prepared by treating the compounds of formula (10.3) with a reducing agent, using the procedures taught in Scheme IV, Step B.

In Step CC (Scheme V), compounds of formula (10.7) can be prepared by reacting compounds of formula (10.5) with sodium nitrite (NaNO₂) in concentrated aqueous HCl at temperatures ranging from about −10° C. to 0° C. for about 2 h or more, then treating the reaction mixture with phosphorous acid (H₃PO₂) at 0° C. for 4 h or more.

In Step DD (Scheme V), compounds of formula (10.9) can be prepared by reacting compounds of formula (10.7) with concentrated aqueous HCl at about 85° C. for about 18 h or more. Compound (10.9) can be reacted using the same procedures described in Scheme IV for treating compound (5.0) and (6.0) and subsequent intermediates therefrom, in order to obtain the desired compounds of formula (1.0).

In Step EE (Scheme V), compounds of formula (10.8) can be prepared by reacting compound of formula (10.7) with NaIO₄and RuO₂in acetonitrile and water for about 18 to 24 h or more at 25° C.

In Step FF (Scheme V), compounds of formula (5.01) wherein X=CH can be prepared by reacting compounds of the formula (10.9) under reducing conditions. Compound (10.9) can be reacted with an alkyl-metal hydride, such as diisobutyl aluminum hydride, in a solvent, such as toluene, at temperatures from about 0° to +90° C.

In Step GG (Scheme V), compounds of formula (1.0) can be prepared using the methods as described in Scheme I, hereinbefore.

In Step OO (Scheme V), compounds of formula (6.51) can be prepared by reacting compounds of formula (10.8) with sodium borohydride (NaBH₄) in a solvent such as ethanol/toluene under reflux conditions for 10 minutes or at 25° C. for two hours or more.

In Step PP (Scheme V), compounds of formula (6.71) can be prepared by reacting compounds of formula (6.51) with SOCl₂in a solvent such as CH₂Cl₂at a temperature of about 25° C. for about 4 hours or more.

In Step QQ (Scheme V), compounds of formula (5.01) wherein X=N, can be prepared by reacting compounds (6.71) with an excess amount of the piperazine compound of formula (6.9) in a solvent such as THF at 25° C., or reflux for one hour or more.

Referring to the Schemes IV and V, except as noted otherwise, emperatures can range from 0° to 100° C., or reflux of the reaction mixture and mounts of the reagents (e.g. compound 2.6) can range from 1 to about 10 moles per mole of reactant (e.g. compound 5.0 or 6.0).

The following preparative examples are intended to exemplify selected tarting materials for preparing compounds of the present invention.

PREPARATIVE EXAMPLE 1

Combine 15 g (38.5 mmol) of 4-(8-chloro-3-bromo-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine-1-carboxylic acid ethyl ester (as taught in Preparative Example 47 of PCT/US 94/11392) and 150 mL of concentrated H₂SO₄at −5° C., then add 3.89 g (38.5 mmol) of KNO₃and stir for 4 hours. Pour the mixture into 3 L of ice and basify with 50% NaOH (aqueous). Extract with CH₂Cl₂, dry over MgSO₄, then filter and concentrate in vacuo to a residue. Recrystallize the residue from acetone to give 6.69 g of the product.

Combine 6.69 g (13.1 mmol) of the product of Step A and 100 mL of 85% EtOH/water, then add 0.66 g (5.9 mmol) of CaCl₂and 6.56 g (117.9 mmol) of Fe and heat the mixture at reflux overnight. Filter the hot reaction mixture through Celite® and rinse the filter cake with hot EtOH. Concentrate the filtrate in vacuo to give 7.72 g of the product.

Combine 7.70 g of the product of Step B and 35 mL of HOAc, then add 45 mL of a solution of Br₂in HOAc and stir the mixture at room temperature overnight. Add 300 mL of 1 N NaOH (aqueous), then 75 mL of 50% NaOH (aqueous) and extract with EtOAc. Dry the extract over MgSO₄and concentrate in vacuo to a residue. Chromatograph the residue (silica gel, 20%-30% EtOAc/hexane) to give 3.47 g of the product (along with another 1.28 g of partially purified product).

Combine 0.557 g (5.4 mmol) of t-butyinitrite and 3 mL of DMF, and heat the mixture at to 60°-70° C. Slowly add (dropwise) a mixture of 2.00 g (3.6 mmol) of the product of Step C and 4 mL of DMF, then cool the mixture to room temperature. Add another 0.64 mL of t-butylnitrite at 40° C. and reheat the mixture to 60°-70° C. for 0.5 hrs. Cool to room temperature and pour the mixture into 150 mL of water. Extract with CH₂Cl₂, dry the extract over MgSO₄and concentrate in vacuo to a residue. Chromatograph the residue (silica gel, 10%-20% EtOAc/hexane) to give 0.74 g of the product.

Combine 0.70 g (1.4 mmol) of the product of Step D and 8 mL of concentrated HCl (aqueous) and heat the mixture at reflux overnight. Add 30 mL of 1 N NaOH (aqueous), then 5 mL of 50% NaOH (aqueous) and extract with CH₂Cl₂. Dry the extract over MgSO₄and concentrate in vacuo to give 0.59 g of the title compound.

PREPARATIVE EXAMPLE 2

racemic as well as (+)- and (−)-isomers

Prepare a solution of 8.1 g of the title compound from Preparative Example 7 in toluene and add 17.3 mL of a 1 M solution of DIBAL (diisobutyl aluminum hydride) in toluene. Heat the mixture at reflux and slowly add (dropwise) another 21 mL of 1 M DIBAL/toluene solution over a period of 40 min. Cool the reaction mixture to about 0° C. and add 700 mL of 1 M HCl (aqueous). Separate and discard the organic phase. Wash the aqueous phase with CH₂Cl₂, discard the extract, then basify the aqueous phase by adding 50% NaOH (aqueous). Extract with CH₂Cl₂, dry the extract over MgSO₄and concentrate in vacuo to give 7.30 g of the title compound, which is a racemic mixture of enantiomers.

PREPARATIVE EXAMPLE 3 Separation of Enantiomers

The racemm title compound of Preparative Example 1 is separated by preparative chiral chromatography (Chiralpack AD, 5 cm×50 cm column, using 20% iPrOH/hexane +0.2% diethylamine), to give the (+)-isomer and the (−)-isomer of the title compound. Altenatively, the enantiomers can also be separated by crystallization with an amino acid such as N-acetylphenylalanine.

PREPARATIVE EXAMPLE 6

racemic as well as (+)- and (−)-enantiomer

Combine 40.0 g (0.124 mole) of the starting ketone (as taught in Preparative Example 20 of PCT/US 94/11392) and 200 mL of H₂SO₄and cool to 0° C. Slowly add 13.78 g (0.136 mole) of KNO₃over a period of 1.5 hrs., then warm to room temperature and stir overnight. Work up the reaction using substantially the same procedure as described for Preparative Example 4, Step A. Chromatograph (silica gel, 20%, 30%, 40%, 50% EtOAc/hexane, then 100% EtOAc) to give 28 g of the 9-nitro product, along with a smaller quantity of the 7-nitro product and 19 g of a mixture of the 7-nitro and 9-nitro compounds. MH⁺(9-nitro)=367.

React 28 g (76.2 mmol) of the 9-nitro product of Step A, 400 mL of 85% EtOH/water, 3.8 g (34.3 mmol) of CaCl₂and 38.28 g (0.685 mole) of Fe at 50° C. Heat the mixture at reflux overnight, filter through Celite® and wash the filter cake with 2×200 mL of hot EtOH. Combine the filtrate and washes, and concentrate in vacuo to a residue. Extract the residue with 600 mL of CH₂Cl₂, wash with 300 mL of water and dry over MgSO₄. Filter and concentrate in vacuo to a residue, then chromatograph (silica gel, 30% EtOAc/CH₂Cl₂) to give 24 g of the product.

Combine 13 g (38.5 mmol) of the product of Step B, 140 mL of HOAc and slowly add a solution of 2.95 mL (57.8 mmol) of Br₂in 10 mL of HOAc over a period of 20 min. Stir the reaction mixture at room temperature, then concentrate in vacuo to a residue. Add CH₂Cl₂and water, then adjust to pH=8-9 with 50% NaOH (aqueous). Wash the organic phase with water, then brine and dry over Na₂SO₄. Concentrate in vacuo to give 11.3 g of the product.

Cool 100 mL of concentrated HCl (aqueous) to 0° C., then add 5.61 g (81.4 mmol) of NaNO₂and stir for 10 min. Slowly add (in portions) 11.3 g (27.1 mmol) of the product of Step C and stir the mixture at 0°-3° C. for 2.25 hrs. Slowly add (dropwise) 180 mL of 50% H₃PO₂(aqueous) and allow the mixture to stand at 0° C. overnight. Slowly add (dropwise) 150 mL of 50% NaOH over 30 min., to adjust to pH=9, then extract with CH₂Cl₂. Wash the extract with water, then brine and dry over Na₂SO₄. Concentrate in vacuo to a residue and chromatograph (silica gel, 2% EtOAc/CH₂Cl₂) to give 8.6 g of the product.

Combine 8.6 g (21.4 mmol) of the product of Step D and 300 mL of MeOH and cool to 0°-20° C. Add 1.21 g (32.1 mmol) of NaBH₄and stir the mixture at ˜0° C. for 1 hr. Add another 0.121 g (3.21 mmol) of NaBH₄, stir for 2 hr. at 0° C., then let stand overnight at 0° C. Concentrate in vacuo to a residue then partition the residue between CH₂Cl₂and water. Separate the organic phase and concentrate in vacuo (50° C.) to give 8.2 g of the product.

Combine 8.2 g (20.3 mmol) of the product of Step E and 160 mL of CH₂Cl₂, cool to 0° C., then slowly add (dropwise) 14.8 mL (203 mmol) of SOCl₂over a 30 min. period. Warm the mixture to room temperature and stir for 4.5 hrs., then concentrate in vacuo to a residue, add CH₂Cl₂and wash with 1 N NaOH (aqueous) then brine and dry over Na₂SO₄. Concentrate in vacuo to a residue, then add dry THF and 8.7 g (101 mmol) of piperazine and stir at room temperature overnight. Concentrate in vacuo to a residue, add CH₂Cl₂, and wash with 0.25 N NaOH (aqueous), water, then brine. Dry over Na₂SO₄and concentrate in vacuo to give 9.46 g of the crude product. Chromatograph (silica gel, 5% MeOH/CH₂Cl₂+NH₃) to give 3.59 g of the title compound, as a racemate.

The racemic title compound from Step F (5.7 g) is chromatographed by preparative chiral chromatography (Chiralpack AD, 5 cm×50 cm column, flow rate 100 mL/min) using 30% iPrOH/hexane+0.2% diethylamine, to give 2.88 g of the R-(+)-enantiomer and 2.77 g of the S-(−)-enantiomer of the title compound.

PREPARATIVE EXAMPLE 7

Combine 25.86 g (55.9 mmol) of 4-(8-chloro-3-bromo-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine-1-carboxylic acid ethyl ester and 250 mL of concentrated H₂SO₄at −5° C., then add 4.8 g (56.4 mmol) of NaNO₃and stir for 2 hours. Pour the mixture into 600 g of ice and basify with concentrated NH₄OH (aqueous). Filter the mixture, wash with 300 mL of water, then extract with 500 mL of OH₂Cl₂. Wash the extract with 200 mL of water, dry over MgSO₄, then filter and concentrate in vacuo to a residue. Chromatograph the residue (silica gel, 10% EtOAc/CH₂Cl₂) to give 24.4 g (86% yield) of the product. m.p.=165-167° C.

Combine 20 g (40.5 mmol) of the product of Step A and 200 mL of concentrated H₂SO₄at 20° C., then cool the mixture to 0° C. Add 7.12 g (24.89 mmol) of 1,3-dibromo-5,5-dimethyl-hydantoin to the mixture and stir for 3 hours at 20° C. Cool to 0° C., add an additional 1.0 g (3.5 mmol) of the dibromohydantoin and stir at 20° C. for 2 hours. Pour the mixture into 400 g of ice, basify with concentrated NH₄OH (aqueous) at 0° C., and collect the resulting solid by filtration. Wash the solid with 300 mL of water, slurry in 200 mL of acetone and filter to provide 19.79 g (85.6% yield) of the product.

Combine 25 g (447 mmol) of Fe filings, 10 g (90 mmol) of CaCl₂and a suspension of 20 g (34.19 mmol) of the product of Step B in 700 mL of 90:10 EtOH/water at 50° C. Heat the mixture at reflux overnight, filter through Celite® and wash the filter cake with 2×200 mL of hot EtOH. Combine the filtrate and washes, and concentrate in vacuo to a residue. Extract the residue with 600 mL of CH₂Cl₂, wash with 300 mL of water and dry over MgSO₄. Filter and concentrate in vacuo to a residue, then chromatograph (silica gel, 30% EtOAc/CH₂Cl₂) to give 11.4 g (60% yield) of the product.

Slowly add (in portions) 20 g (35.9 mmol) of the product of Step C to a solution of 8 g (116 mmol) of NaNO₂in 120 mL of concentrated HCl (aqueous) at −10° C. Stir the resulting mixture at 0° C. for 2 hours, then slowly add (dropwise) 150 mL (1.44 mole) of 50% H₃PO₂at 0° C. over a 1 hour period. Stir at 0° C. for 3 hours, then pour into 600 g of ice and basify with concentrated NH₄OH (aqueous). Extract with 2×300 mL of CH₂Cl₂, dry the extracts over MgSO₄, then filter and concentrate in vacuo to a residue. Chromatograph the residue (silica gel, 25% EtOAc/hexanes) to give 13.67 g (70% yield) of the product.

Combine 6.8 g (12.59 mmol) of the product of Step D and 100 mL of concentrated HCl (aqueous) and stir at 85° C. overnight. Cool the mixture, pour it into 300 g of ice and basify with concentrated NH₄OH (aqueous). Extract with 2×300 mL. of CH₂Cl₂, then dry the extracts over MgSO₄. Filter, concentrate in vacuo to a residue, then chromatograph (silica gel, 10% MeOH/EtOAc+2% NH₄OH (aqueous)) to give 5.4 g (92% yield) of the title compound.

PREPARATIVE EXAMPLE 8 racemic as well as (+)- and (−)-enantiomers

Combine 16.6 g (0.03 mole) of the product of Preparative Example 7, Step D, with a 3:1 solution of CH₃CN and water (212.65 mL CH₃CN and 70.8 mL of water) and stir the resulting slurry overnight at room temperature. Add 32.833 g (0.153 mole) of NalO₄and then 0.31 g (2.30 mmol) of RuO₂and stir at room temperature (the addition of RuO₂is accompanied by an exothermic reaction and the temperature climbs from 20° to 30° C.). Stir the mixture for 1.3 hrs. (temperature returned to 25° C. after about 30 min.), then filter to remove the solids and wash the solids with CH₂Cl₂. Concentrate the filtrate in vacuo to a residue and dissolve the residue in CH₂Cl₂. Filter to remove insoluble solids and wash the solids with CH₂Cl₂. Wash the filtrate with water, concentrate to a volume of about 200 mL and wash with bleach, then with water. Extract with 6 N HCl (aqueous). Cool the aqueous extract to 0° C. and slowly add 50% NaOH (aqueous) to adjust to pH=4 while keeping the temperature <30° C. Extract twice with CH₂Cl₂, dry over MgSO₄and concentrate in vacuo to a residue. Slurry the residue in 20 mL of EtOH and cool to 0° C. Collect the resulting solids by filtration and dry the solids in vacuo to give 7.95 g of the product.

Combine 21.58 g (53.75 mmol) of the product of Step A and 500 mL of an anhydrous 1:1 mixture of EtOH and toluene, add 1.43 g (37.8 mmol) of NaBH₄and heat the mixture at reflux for 10 min. Cool the mixture to 0° C., add 100 mL of water, then adjust to pH=4-5 with 1 M HCl (aqueous) while keeping the temperature <10° C. Add 250 mL of EtOAc and separate the layers. Wash the organic layer with brine (3×50 mL) then dry over Na₂SO₄. Concentrate in vacuo to a residue (24.01 g) and chromatograph the residue (silica gel, 30% hexane/CH₂Cl₂) to give the product. Impure fractions were purified by rechromatography. A total of 18.57 g of the product is obtained.

Combine 18.57 g (46.02 mmol) of the product of Step B and 500 mL of CHCl₃, then add 6.70 mL (91.2 mmol) of SOCl₂, and stir the mixture at room temperature for 4 hrs. Add a solution of 35.6 g (0.413 mole) of piperazine in 800 mL of THF over a period of 5 min. and stir the mixture for 1 hr. at room temperature. Heat the mixture at reflux overnight, then cool to room temperature and dilute the mixture with 1 L of CH₂Cl₂. Wash with water (5×200 mL), and extract the aqueous wash with CHCl₃(3×100 mL). Combine all of the organic solutions, wash with brine (3×200 mL) and dry over MgSO₄. Concentrate in vacuo to a residue and chromatograph (silica gel, gradient of 5%, 7.5%, 10% MeOH/CH₂Cl₂+NH₄OH) to give 18.49 g of the title compound as a racemic mixture.

The racemic title compound of Step C is separated by preparative chiral chromatography (Chiralpack AD, 5 cm×50 cm column, flow rate 100 mL/min., 20% iPrOH/hexane+0.2% diethylamine), to give 9.14 g of the (+)-enantiomer and 9.30 g of the (−)-enantiomer.

PREPARATIVE EXAMPLE 9

racemic as well as (+)- and (−)-enantiomer

Combine 13 g (33.3 mmol) of the title compound from Preparative Example 7, and 300 mL of toluene at 20° C., then add 32.5 mL (32.5 mmol) of a 1 M solution of DIBAL in toluene. Heat the mixture at reflux for 1 hr., cool to 20° C., add another 32.5 mL of 1 M DIBAL solution and heat at reflux for 1 hr. Cool the mixture to 20° C. and pour it into a mixture of 400 g of ice, 500 mL of EtOAc and 300 mL of 10% NaOH (aqueous). Extract the aqueous layer with CH₂Cl₂(3×200 mL), dry the organic layers over MgSO₄, then concentrate in vacuo to a residue. Chromatograph (silica gel, 12% MeOH/CH₂Cl₂+4% NH₄OH) to give 10.4 g of the title compound as a racemate.

The racemic title compound of Step A is separated by preparative chiral chromatography (Chiralpack AD, 5 cm×50 cm column, using 5% iPrOH/hexane+0.2% diethylamine), to give the (+)-enantiomer and the (−)-enantiomer of the title compound.

PREPARATIVE EXAMPLE 10

Combine 15 g (38.5 mmol) of 4-(8-chloro-3-bromo-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine-1-carboxylic acid ethyl ester and 150 mL of concentrated H₂SO₄at −5° C., then add 3.89 g (38.5 mmol) of KNO₃and stir for 4 hours. Pour the mixture into 3 L of ice and basify with 50% NaOH (aqueous). Extract with CH₂Cl₂, dry over MgSO₄, then filter and concentrate in vacuo to a residue. Recrystallize the residue from acetone to give 6.69 g of the product.

Combine 6.69 g (13.1 mmol) of the product of Step A and 100 mL of 85% EtOH/water, then add 0.66 g (5.9 mmol) of CaCl₂and 6.56 g (117.9 mmol) of Fe and heat the mixture at reflux overnight. Filter the hot reaction mixture through Celite®) and rinse the filter cake with hot EtOH. Concentrate the filtrate in vacuo to give 7.72 g of the product.

Dissolve 9.90 g (18.9 mmol) of the product of Step B, in 150 mL CH₂Cl₂and 200 mL of CH₃CN and heat to 60° C. Add 2.77 g (20.8 mmol) N-chlorosuccinimide and heat to reflux for 3 h., monitoring the reaction by TCL (30% EtOAc/H₂O). Add an additional 2.35 g (10.4 mmol) of N-chlorosuccinimide and reflux an additional 45 min. Cool the reaction mixture to room temperature and extract with 1 N NaOH and CH₂Cl₂. Dry the CH₂Cl₂layer over MgSO₄, filter and purify by flash chromatography (1200 mL normal phase silica gel, eluting with 30% EtOAc/H₂O) to obtain 6.24 g of the desired product. M.p. 193-195.4° C.

To 160 mL of conc. HCl at −10° C. add 2.07 g (30.1 mmol) NaNO₂and stir for 10 min. Add 5.18 g (10.1 mmol) of the product of Step A and warm the reaction mixture from −10° C. to 0° C. for 2 h. Cool the reaction to −10° C., add 100 mL H₃PO₂and let stand overnight. To extract the reaction mixture, pour over crushed ice and basify with 50% NaOH/CH₂Cl₂. Dry the organic layer over MgSO₄, filter and concentrate to dryness. Purify by flash chromatography (600 mL normal phase silica gel, eluting with 20% EtOAc/hexane) to obtain 3.98 g of product.

Dissolve 3.9 g of the product of Step D in 100 mL conc. HCl and reflux overnight. Cool the mixture, basify with 50% w/w NaOH and extract the resultant mixture with CH₂Cl₂. Dry the CH₂Cl₂layer over MgSO₄, evaporate the solvent and dry under vacuum to obtain 3.09 g of the desired product.

Using a procedure similar to that described in Preparative Example 8, obtain 1.73 g of the desired product, m.p. 169.6-170.1° C.; [a]_D ²⁵=+48.2° (c=1, MeOH). MH⁺=425.

ASSAYS

1. In vitro enzyme assays: FPT IC₅₀(inhibition of farnesyl protein transferqase, in vitro enzyme assay) are determined by the methods disclosed in WO/10515 or WO 95/10516. The data demonstrate that the compounds of the invention are inhibitors of Ras-CVLS farnesylation by partially purified rat brain farnesyl protein transferase (FPT). The data also show that there are compounds of the invention which can be considered as potent (IC₅₀<10 μM) inhibitors of Ras-CVLS farnesylation by partially purified rat brain FPT.

2. Cell-based assay. COS IC₅₀values refer to the COS cells activity inhibition of Ras processing, are determined by the methods disclosed in WO/10515 or WO 95/10516.


		H-ras FPT
	Example No.	IC₅₀(μM)

	1	0.0080
	2	0.1640
	3	0.0260
	4	0.0070
	5	0.0154
	6	0.0320
	7	0.1100
	8	0.3200
	9	0.0340
	10	0.0890
	11	0.0320
	12	0.1790
	13	0.0850
	14	0.2760

For preparintg pharmaceutical compositions from the compounds, described by this invention, inert, pharmaceutically acceptable carriers can be either solid or liquid. Solid form preparations include powders, tablets, dispersible granules, capsules, cachets and suppositories. The powders and tablets may be comprised of from about 5 to about 70 percent active ingredient. Suitable solid carriers are known in the art, e.g. magnesium carbonate, magnesium stearate, talc, sugar, lactose. Tablets, powders, cachets and capsules can be used as solid dosage forms suitable for oral administration.

For preparing suppositories, a low melting wax such as a mixture of fatty acid glycerides or cocoa butter is first melted, and the active ingredient is dispersed homogeneously therein as by stirring. The molten homogeneous mixture is then poured into convenient sized molds, allowed to cool and thereby solidify.

Liquid form preparations include solutions, suspensions and emulsions. As an example may be mentioned water or water-propylene glycol solutions for parenteral injection.

Liquid form preparations may also include solutions for intranasal administration.

Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be in combination with a pharmaceutically acceptable carrier, such as an inert compressed gas.

Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for either oral or parenteral administration. Such liquid forms include solutions, suspensions and emulsions.

The compounds of the invention may also be deliverable transdermally. The transdermal compositions can take the form of creams, lotions, aerosols and/or emulsions and can be included in a transdermal patch of the matrix or reservoir type as are conventional in the art for this purpose.

Preferably the compound is administered orally.

Preferably, the pharmaceutical preparation is in unit dosage form. In such form, the preparation is subdivided into unit doses containing appropriate quantities of the active component, e.g., an effective amount to achieve the desired purpose.

The quantity of active compound in a unit dose of preparation may be varied or adjusted from about 0.1 mg to 1000 mg, more preferably from about 1 mg. to 300 mg, according to the particular application.

The actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage for a particular situation is within the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small increments until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day if desired.

The amount and frequency of administration of the compounds of the invention and the pharmaceutically acceptable salts thereof will be regulated according to the judgment of the attending clinician considering such factors as age, condition and size of the patient as well as severity of the symptoms being treated. A typical recommended dosage regimen is oral administration of from 10 mg to 2000 mg/day preferably 10 to 1000 mg/day, in two to four divided doses to block tumor growth. The compounds are non-toxic when administered within this dosage range.

The following are examples of pharmaceutical dosage forms which contain a compound of the invention. The scope of the invention in its pharmaceutical composition aspect is not to be limited by the examples provided.

PHARMACEUTICAL DOSAGE FORM EXAMPLES Example A Tablets


No.	Ingredients	mg/tablet	mg/tablet

1.	Active compound	100	500
2.	Lactose USP	122	113
3.	Corn Starch, Food Grade,	30	40
	as a 10% paste in
	Purified Water
4.	Corn Starch, Food Grade	45	40
5.	Magnesium Stearate	3	7
	Total	300	700

Method of Manufacture

Mix Item Nos. 1 and 2 in a suitable mixer for 10-15 minutes. Granulate the mixture with Item No. 3. Mill the damp granules through a coarse screen (e.g., ¼″, 0.63 cm) if necessary. Dry the damp granules. Screen the dried granules if necessary and mix with Item No. 4 and mix for 10-15 minutes. Add Item No. 5 and mix for 1-3 minutes. Compress the mixture to appropriate size and weigh on a suitable tablet machine.

Example B Capsules


No.	Ingredient	mg/capsule	mg/capsule

1.	Active compound	100	500
2.	Lactose USP	106	123
3.	Corn Starch, Food Grade	40	70
4.	Magnesium Stearate NF	7	7
	Total	253	700

Method of Manufacture

Mix Item Nos. 1, 2 and 3 in a suitable blender for 10-15 minutes. Add Item No. 4 and mix for 1-3 minutes. Fill the mixture into suitable two-piece hard gelatin capsules on a suitable encapsulating machine.

While the present invention has been described in conjunction with the specific embodiments set forth above, many alternatives, modifications and variations thereof will be apparent to those of ordinary skill in the art. All such alternatives, modifications and variations are intended to fall within the spirit and scope of the present invention.

Claims

What is claimed is:

1. A compound selected from:

2. The compound of claim 1 having the formula:

3. The compound of claim 1 having the formula:

4. The compound of claim 1 having the formula:

5. The compound of claim 1 having the formula:

6. The compound of claim 1 having the formula:

7. The compound of claim 1 having the formula:

8. The compound of claim 1 having the formula:

9. The compound of claim 1 having the formula:

10. The compound of claim 1 having the formula:

11. The compound of claim 1 having the formula:

12. The compound of claim 1 having the formula:

13. The compound of claim 1 having the formula:

14. The compound of claim 1 having the formula:

15. The compound of claim 1 having the formula:

16. A pharmaceutical composition comprising an effective amount of compound of claim 1 in combination with a pharmaceutically acceptable carrier.

17. A method of inhibiting farnesyl protein transferase in a patient in need thereof comprising administering to said patient an effective amount of a compound of claim 1.

18. A method of inhibiting pancreatic tumor cells, lung cancer cells, myeloid leukemia tumor cells, thyroid follicular tumor cells, myelodysplastic tumor cells, epidermal carcinoma tumor cells, bladder carcinoma tumor cells, prostate tumor cells, breast tumor cells or colon tumors cells in a patient in need thereof by the inhibition of farnesyl protein transferase comprising administering to said patient an effective amount of a compound of claim 1.